Linked Data
ClinVar Variation Id:
427933
dbSNP Id:
rs372770167
gnomAD v2:
2-232079625-C-T
gnomAD v3:
2-231214912-C-T
gnomAD v4:
2-231214912-C-T
PubMed:
PMID:28625504
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.231214912C>T , CM000664.2:g.231214912C>T | GRCh38 |
| NC_000002.11:g.232079625C>T , CM000664.1:g.232079625C>T | GRCh37 |
| NC_000002.10:g.231787869C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436339.6:c.259C>T | ENSP00000392086.2:p.Arg87Ter | |
| ENST00000440107.6:c.259C>T | ENSP00000387391.2:p.Arg87Ter | |
| ENST00000482392.2:n.363C>T | ||
| ENST00000682002.1:c.259C>T | ENSP00000507152.1:p.Arg87Ter | |
| ENST00000682027.1:n.368C>T | ||
| ENST00000682030.1:c.256C>T | ENSP00000508117.1:p.Arg86Ter | |
| ENST00000682100.1:c.259C>T | ENSP00000507066.1:p.Arg87Ter | |
| ENST00000682233.1:n.570C>T | ||
| ENST00000682264.1:c.259C>T | ENSP00000507212.1:p.Arg87Ter | |
| ENST00000682334.1:c.259C>T | ENSP00000507763.1:p.Arg87Ter | |
| ENST00000682367.1:c.256C>T | ENSP00000507235.1:p.Arg86Ter | |
| ENST00000682751.1:n.566C>T | ||
| ENST00000683040.1:c.259C>T | ENSP00000507817.1:p.Arg87Ter | |
| ENST00000683063.1:c.133C>T | ENSP00000507407.1:p.Arg45Ter | |
| ENST00000683107.1:n.356C>T | ||
| ENST00000683112.1:c.259C>T | ENSP00000507357.1:p.Arg87Ter | |
| ENST00000683165.1:n.405C>T | ||
| ENST00000683271.1:c.259C>T | ENSP00000507513.1:p.Arg87Ter | |
| ENST00000683275.1:c.259C>T | ENSP00000506823.1:p.Arg87Ter | |
| ENST00000683321.1:c.259C>T | ENSP00000508154.1:p.Arg87Ter | |
| ENST00000683553.1:c.259C>T | ENSP00000506860.1:p.Arg87Ter | |
| ENST00000683575.1:c.259C>T | ENSP00000507743.1:p.Arg87Ter | |
| ENST00000683629.1:c.259C>T | ENSP00000507960.1:p.Arg87Ter | |
| ENST00000683702.1:c.259C>T | ENSP00000507686.1:p.Arg87Ter | |
| ENST00000683814.1:n.570C>T | ||
| ENST00000683966.1:c.259C>T | ENSP00000507325.1:p.Arg87Ter | |
| ENST00000684011.1:n.364C>T | ||
| ENST00000684051.1:c.259C>T | ENSP00000507854.1:p.Arg87Ter | |
| ENST00000684368.1:c.259C>T | ENSP00000508353.1:p.Arg87Ter | |
| ENST00000684432.1:c.259C>T | ENSP00000508405.1:p.Arg87Ter | |
| ENST00000684565.1:c.259C>T | ENSP00000507599.1:p.Arg87Ter | |
| ENST00000684718.1:c.259C>T | ENSP00000507543.1:p.Arg87Ter | |
| ENST00000611582.5:c.259C>T MANE Select | ENSP00000484804.1:p.Arg87Ter | |
| ENST00000349938.8:c.259C>T | ENSP00000258417.5:p.Arg87Ter | |
| ENST00000440107.5:c.259C>T | ENSP00000387391.1:p.Arg87Ter | |
| ENST00000482392.1:n.356C>T | ||
| ENST00000611582.4:c.259C>T | ENSP00000484804.1:p.Arg87Ter | |
| ENST00000614261.4:c.259C>T | ENSP00000484241.1:p.Arg87Ter | |
| NM_001271466.2:c.259C>T | NP_001258395.1:p.Arg87Ter | |
| NM_001291656.1:c.259C>T | NP_001278585.1:p.Arg87Ter | |
| NM_025139.5:c.259C>T | NP_079415.3:p.Arg87Ter | |
| XM_011511905.1:c.259C>T | XP_011510207.1:p.Arg87Ter | |
| XM_011511906.1:c.259C>T | XP_011510208.1:p.Arg87Ter | |
| XM_011511907.1:c.259C>T | XP_011510209.1:p.Arg87Ter | |
| XM_011511908.1:c.259C>T | XP_011510210.1:p.Arg87Ter | |
| XM_011511909.1:c.259C>T | XP_011510211.1:p.Arg87Ter | |
| XM_011511910.1:c.259C>T | XP_011510212.1:p.Arg87Ter | |
| XM_011511911.1:c.259C>T | XP_011510213.1:p.Arg87Ter | |
| XM_011511912.1:c.259C>T | XP_011510214.1:p.Arg87Ter | |
| XM_011511913.1:c.259C>T | XP_011510215.1:p.Arg87Ter | |
| XM_011511914.1:c.259C>T | XP_011510216.1:p.Arg87Ter | |
| XM_011511915.1:c.259C>T | XP_011510217.1:p.Arg87Ter | |
| XM_011511916.1:c.259C>T | XP_011510218.1:p.Arg87Ter | |
| XM_011511917.1:c.259C>T | XP_011510219.1:p.Arg87Ter | |
| XM_011511918.1:c.259C>T | XP_011510220.1:p.Arg87Ter | |
| XM_011511920.1:c.259C>T | XP_011510222.1:p.Arg87Ter | |
| XR_923031.1:n.371C>T | ||
| XR_923032.1:n.371C>T | ||
| NM_001271466.3:c.259C>T | NP_001258395.1:p.Arg87Ter | |
| NM_001352754.1:c.259C>T | NP_001339683.1:p.Arg87Ter | |
| NM_001352755.1:c.259C>T | NP_001339684.1:p.Arg87Ter | |
| NM_001352756.1:c.259C>T | NP_001339685.1:p.Arg87Ter | |
| NM_001352757.1:c.259C>T | NP_001339686.1:p.Arg87Ter | |
| NM_001352758.1:c.259C>T | NP_001339687.1:p.Arg87Ter | |
| NM_001352759.1:c.259C>T | NP_001339688.1:p.Arg87Ter | |
| NR_148040.1:n.453C>T | ||
| XM_011511908.2:c.259C>T | XP_011510210.1:p.Arg87Ter | |
| XM_011511909.2:c.259C>T | XP_011510211.1:p.Arg87Ter | |
| XM_011511913.2:c.259C>T | XP_011510215.1:p.Arg87Ter | |
| XM_011511914.2:c.259C>T | XP_011510216.1:p.Arg87Ter | |
| XM_011511915.2:c.259C>T | XP_011510217.1:p.Arg87Ter | |
| XM_011511916.2:c.259C>T | XP_011510218.1:p.Arg87Ter | |
| XM_017005021.1:c.259C>T | XP_016860510.1:p.Arg87Ter | |
| XM_017005022.1:c.259C>T | XP_016860511.1:p.Arg87Ter | |
| XM_017005024.1:c.259C>T | XP_016860513.1:p.Arg87Ter | |
| XM_017005025.1:c.259C>T | XP_016860514.1:p.Arg87Ter | |
| NM_001271466.4:c.259C>T | NP_001258395.2:p.Arg87Ter | |
| NM_001291656.2:c.259C>T | NP_001278585.2:p.Arg87Ter | |
| NM_001352754.2:c.259C>T MANE Select | NP_001339683.2:p.Arg87Ter | |
| NM_001352755.2:c.259C>T | NP_001339684.2:p.Arg87Ter | |
| NM_001352756.2:c.259C>T | NP_001339685.2:p.Arg87Ter | |
| NM_001352757.2:c.259C>T | NP_001339686.2:p.Arg87Ter | |
| NM_001352758.2:c.259C>T | NP_001339687.2:p.Arg87Ter | |
| NM_001352759.2:c.259C>T | NP_001339688.2:p.Arg87Ter | |
| NM_025139.6:c.259C>T | NP_079415.4:p.Arg87Ter | |
| NR_148040.2:n.368C>T |